A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5560331



Internal ID333341
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:38695377..38744597hg38UCSC Ensembl
chr18:36275341..36324561hg19UCSC Ensembl
Cytoband18q12.2
Allele length
AssemblyAllele length
hg3849221
hg1949221
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17717477
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5560331
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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